PH12015502425A1 - Novel compounds for selective histone deacetylase inhibitors, and pharmeceutical composition comprising the same - Google Patents

Novel compounds for selective histone deacetylase inhibitors, and pharmeceutical composition comprising the same

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Publication number
PH12015502425A1
PH12015502425A1 PH12015502425A PH12015502425A PH12015502425A1 PH 12015502425 A1 PH12015502425 A1 PH 12015502425A1 PH 12015502425 A PH12015502425 A PH 12015502425A PH 12015502425 A PH12015502425 A PH 12015502425A PH 12015502425 A1 PH12015502425 A1 PH 12015502425A1
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PH
Philippines
Prior art keywords
histone deacetylase
same
urea derivatives
novel compounds
deacetylase inhibitors
Prior art date
Application number
PH12015502425A
Other versions
PH12015502425B1 (en
Inventor
Lee Changsik
Yang Hyun-Mo
Choi Hojin
Kim Dohoon
Kim Soyoung
Ha Nina
Lim Hyojin
Ko Eunhee
Yoon Seongae
Bae Daekwon
Original Assignee
Chong Kun Dang Pharm Corp
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Publication date
Application filed by Chong Kun Dang Pharm Corp filed Critical Chong Kun Dang Pharm Corp
Publication of PH12015502425A1 publication Critical patent/PH12015502425A1/en
Publication of PH12015502425B1 publication Critical patent/PH12015502425B1/en

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    • C07D295/20—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof
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    • C07D309/08—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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Abstract

The present invention relates to novel urea derivatives and, more particularly, to novel urea derivatives with histone deacetylase (HDAC) inhibitory activity, isomers thereof, pharmaceutically acceptable salts thereof, their use for the preparation of a medicaments comprising the same, a pharmaceutical composition comprising the same, a treatment method using the composition, and a method for preparing novel urea derivatives. The novel urea derivatives as selective histone deacetylase (HDAC) inhibitors are effective for the treatment of histone deacetylase-mediated diseases such as malignant tumors, inflammatory diseases, rheumatoid arthritis, neurodegeneration, etc.
PH12015502425A 2013-04-29 2015-10-21 Novel compounds for selective histone deacetylase inhibitors, and pharmeceutical composition comprising the same PH12015502425B1 (en)

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